rs3180380
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs3180380(C;C) |
Make rs3180380(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356712 |
Gene | HLA-B, MIR6891 |
is a | snp |
is | mentioned by |
dbSNP | rs3180380 |
dbSNP (classic) | rs3180380 |
ClinGen | rs3180380 |
ebi | rs3180380 |
HLI | rs3180380 |
Exac | rs3180380 |
Gnomad | rs3180380 |
Varsome | rs3180380 |
LitVar | rs3180380 |
Map | rs3180380 |
PheGenI | rs3180380 |
Biobank | rs3180380 |
1000 genomes | rs3180380 |
hgdp | rs3180380 |
ensembl | rs3180380 |
geneview | rs3180380 |
scholar | rs3180380 |
rs3180380 | |
pharmgkb | rs3180380 |
gwascentral | rs3180380 |
openSNP | rs3180380 |
23andMe | rs3180380 |
SNPshot | rs3180380 |
SNPdbe | rs3180380 |
MSV3d | rs3180380 |
GWAS Ctlg | rs3180380 |
GMAF | 0.1538 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs3180380(C;C) rs3180380(T;T) |
Alt | rs3180380(C;C) rs3180380(T;T) |
Reference | Rs3180380(G;G) |
Significance | Histocompatibility |
Disease | |
Variation | info |
Gene | HLA-B |
CLNDBN | |
Reversed | 1 |
HGVS | NC_000006.11:g.31324489C>A; NC_000006.11:g.31324489C>G |
CLNSRC | |
CLNACC |